Biotechnology Jobs

• Slough
• On-site
• Mid-level
• Permanent

Performs routine, non-routine and stability testing of biologic drug substances in a client's Analytical Service Department, running ELISA, cell-based and Biacore assays and capturing data in laboratory software and electronic notebooks. Generates and reviews GMP-compliant documentation, SOPs and protocols, supports method development and validation, and handles out-of-specification investigations while liaising with internal and external clients.

Biacore · Vi-Cell · Microsoft Office

• Wolverhampton
• Mid-level · manages people
• Permanent

Responsible for managing a pathology laboratory's day-to-day operations, ensuring compliance with ISO 17025, UKAS and retail quality standards. Duties include safety and COSHH compliance, equipment calibration, audit leadership, KPI monitoring, and developing Team Leaders while maintaining 7-day shift coverage.

LIMS · Microsoft Excel · Microsoft Word

• Swindon
• Entry level
• Internship

Support the QC Chemistry team by performing routine analytical testing of incoming goods, intermediates and finished products under cGMP conditions. Duties include stock control of reagents and reference standards, equipment checks, calibration and preventative maintenance, reagent preparation, glassware washing, waste disposal and maintaining technical documentation and training records.

pH Meters · Balances

• Oxford
• Hybrid · 4 days in office
• Lead · manages people
• Permanent

Lead a team building software platforms that integrate scientific workflows, AI capabilities, robotics and laboratory automation. The role blends team leadership with hands-on engineering: setting technical direction, organising delivery, designing systems and writing production code. Works closely with scientists, product teams, hardware engineers and AI specialists, with practical agentic AI knowledge required.

• Milton Keynes
• Remote
• £37,500 pa
• Mid-level
• Permanent

Provide first-line remote technical support for specialist laboratory analysers and medical devices, diagnosing faults using remote-access tools such as RDP, VNC and augmented reality. Work with laboratory staff, field service engineers and product specialists to resolve issues and minimise on-site visits, while training users and maintaining service records.

RDP · VNC · Augmented Reality

• Oxford
• Hybrid · 3–4 days in office
• Director

As an individual contributor in the Clinical Pharmacology group, you will develop quantitative strategies for dose selection, PK/PD characterization and regimen optimization across oncology, immunology and rare disease programs. You will partner with Pharmacometrics and QSP colleagues, represent CQP on program teams, and contribute to regulatory documentation and interactions.

R · Phoenix WinNonlin · NONMEM +2

• Buckinghamshire
• On-site
• £34,000 – £35,000 pa

Combines technical applications support with outbound sales for a Life Sciences SME supplying cell biology and recombinant protein products. You'll troubleshoot customer issues, recommend products, follow up leads and quotations, and proactively develop new business by phone and email, working in a small team.

• Edinburgh
• Lead

Designs, delivers and interprets complex molecular and cellular biology studies for drug discovery and translational research, combining hands-on lab work with technical direction across client programmes. Provides scientific leadership on multiple projects, evaluates new technologies and supports colleagues, working with mammalian cell cultures and advanced cellular systems.

• Stevenage
• Hybrid

Predominantly laboratory-based role planning, executing and interpreting LC-MS and LC-MS/MS experiments to characterise biopharmaceutical molecules. You will develop and troubleshoot analytical methods, investigate product quality attributes and post-translational modifications, and support early-phase programmes through forced degradation and comparability studies. Works across Discovery and CMC Development teams, with hybrid working available.

Protein Metrics · JMP · SIMCA

• Cambridge
• On-site
• £20 – £24 ph
• Mid-level
• Temporary

Undertake routine and specialist microbiological and molecular investigations across bacteriology, Containment Level 3, serology, chlamydia and molecular diagnostics, interpreting and reporting results. Operate and maintain automated analysers, manage consumables and lab IT systems, and contribute to quality management, audits and SOP development. Based at Addenbrooke's Hospital within UKHSA's Public Health Microbiology team.

UKAS · HSE

• Guildford
• Mid-level
• Permanent

Hands-on laboratory role analysing pharmaceutical samples including APIs, medicines, herbal products and packaging for MHRA Laboratories. Uses HPLC, GC, GC/LC-MS, IR, Raman, UV, dissolution and wet chemistry, with responsibility for drafting reports, validating data, equipment calibration and maintaining an ISO/IEC 17025 quality system. Works within a team of around 30 analytical scientists, independently coordinating project workloads.

Microsoft Word · Microsoft Excel

• Cardiff
• On-site
• £200 – £305 pd
• Contract

Field-based, customer-facing role supporting diagnostic systems in laboratories across South Wales. You provide hands-on product and application support, train lab staff, troubleshoot technical issues, and assist with system implementation and optimisation, working alongside technical and engineering specialists. Requires travel with occasional overnight stays.

• United Kingdom
• £55,000 – £70,000 pa

This role involves leading in-vitro toxicology studies within a regulated preclinical environment, focusing on assay development and execution for product safety assessment. The scientist will apply advanced cell-based methods including Neutral Red, Ames, and micronucleus assays, interpret complex biological data, and support regulatory submissions. Collaboration with internal teams and external partners is key, alongside method validation and scientific reporting in a quality-assured laboratory setting.

• Swindon
• Lead · manages people

Leads a team of scientific officers performing GMP QC Chemistry analysis of incoming goods, in-process, intermediate, stability and finished product samples. Acts as first escalation point for technical, compliance and personnel issues, manages batch release, stability studies, documentation and audits, and deputises for the QC Manager. Requires extensive instrumental and traditional analytical experience plus 2+ years of team leadership.

• Aylesbury
• £23 ph

Job summaryWe have an exciting opportunity for a Biomedical Scientist Microbiology at Buckinghamshire Healthcare NHS Trust to join the Microbiology Department at Stoke Mandeville Hospital. You will be responsible for performing specialist microbiology and serology investigations in accordance with departmental…